Comment by the__alchemist
Comment by the__alchemist 2 days ago
An (agarose?) gel.
There are partial holes in at at one end. You insert a small amount of dyed DNA (etc) containing solution each. Apply an electrical potential across the gel. DNA gradually moves along. Smaller DNA fragments move faster. So, at a given time, you can coarsely measure fragment size of a given sample. Your absolute scale is given by "standards", aka "ladders" that have samples of multiple, known sizes.
The paper authors cheated (allegedly) by copy + pasting images of the gel. This is what was caught, so it implies they may have made up some or all results in this and other papers.
Close - this is a SDS-PAGE gel, and you run it using proteins. The bands in the first two rows are from a western blot (gel is transferred to a membrane), where you use antibodies against those specific proteins to detect them. The Pon S row is Ponceau S, a dye that non-specifically detects all proteins - so it's used as a loading control, to make sure that the same amount of total protein is loaded in each lane of the gel.